×
CUI:
C0013604
Disease:
Edema
Edema
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
126
1
0.100
None
0
Erythema
phenotype
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Disease or Syndrome
227
8
0.100
None
0
Iron-Refractory Iron Deficiency Anemia
disease
Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
51
36
0.100
None
0
Hypertriglyceridemia
phenotype
Nutritional and Metabolic Diseases
Disease or Syndrome
340
169
0.100
None
0
Decreased liver function
phenotype
Finding
59
5
0.100
None
0
Eczema
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
863
368
0.100
None
0
Photosensitivity of skin
phenotype
Skin and Connective Tissue Diseases
Pathologic Function
91
3
0.100
None
0
Cholelithiasis
disease
Digestive System Diseases
Disease or Syndrome
252
90
0.100
None
0
Pruritus
phenotype
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Finding
107
2
0.100
None
0
Anemia, Hemolytic
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
154
31
0.100
None
0
Childhood onset
phenotype
Finding
56
0.100
None
0
Adenocarcinoma of colon
disease
Digestive System Diseases; Neoplasms
Neoplastic Process
406
10
0.010
None
1.000
1
1993
1993
Bovine Protoporphyria
disease
Disease or Syndrome
1
0.020
None
1.000
2
1982
1998
Skin-ache syndrome
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
1
0.010
None
1.000
1
1998
1998
Fibrosis
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
184
0.300
None
1.000
1
1999
1999
Cirrhosis
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
919
110
0.400
None
1.000
1
1999
1999
Bile Duct Diseases
group
Digestive System Diseases
Disease or Syndrome
9
0.300
None
1.000
1
1999
1999
Variegate Porphyria
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
21
24
0.030
None
1.000
3
1977
2002
Myeloid Leukemia
disease
Neoplasms
Neoplastic Process
385
7
0.010
None
1.000
1
2002
2002
Acute intermittent porphyria
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
103
68
0.010
None
1.000
1
2002
2002
Acute interstitial pneumonia
disease
Respiratory Tract Diseases
Disease or Syndrome
88
8
0.010
None
1.000
1
2002
2002
Porphyria Cutanea Tarda
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
30
39
0.010
None
1.000
1
2002
2002
Porphyrias, Hepatic
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
7
0.210
None
1.000
2
1984
2004
Von Hippel-Lindau Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
Disease or Syndrome
174
187
0.010
None
1.000
1
2004
2004
Hepatobiliary disease
disease
Digestive System Diseases
Disease or Syndrome
14
0.020
None
1.000
2
1992
2006